分子内力
共轭微孔聚合物
光催化
材料科学
光化学
聚合物
阳离子聚合
电子转移
离子键合
化学工程
离子液体
微型多孔材料
共轭体系
化学
高分子化学
有机化学
催化作用
工程类
离子
复合材料
作者
Wenling Zhao,Dong Zhai,Chengcheng Liu,Daoyuan Zheng,Hao Wu,Lei Sun,Zhen Li,Tie Yu,Wei Zhou,Xu Fang,Hongjun Zhu,Keli Han,Zuoli He,Wei Deng
标识
DOI:10.1016/j.apcatb.2021.120719
摘要
Efficient solar energy-driven conversion of CO2 to valuable chemicals is challenging. Here we design an imidazolium-based ionic conjugated microporous polymer (ImI-CMP), which unblocks readily intramolecular charge transfer and triggers CO2 photoreduction. Under visible light irradiation, ImI-CMP incorporated with Co (II) species exhibits a high CO production rate of 2953 μmol g−1 h−1 and a turnover frequency of 30.8 h−1; these numbers are competitive to that of the best porous organic polymers. The mechanism studies reveal that two factors play key roles in the outstanding photocatalytic performance. First, the imidazolium motifs on the ImI-CMP enhance the activation of CO2. Second, π-conjugation structure and the built-in electric field allow ultrafast intramolecular photoinduced electron transfer in the ImI-CMP. This work provides a new strategy for designing high-performance organic photocatalysts for CO2 reduction by combining cationic imidazolium motifs and π-conjugation structures.
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